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JPH0437151B2 - - Google Patents
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JPH0437151B2 - - Google Patents

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Publication number
JPH0437151B2
JPH0437151B2 JP1250705A JP25070589A JPH0437151B2 JP H0437151 B2 JPH0437151 B2 JP H0437151B2 JP 1250705 A JP1250705 A JP 1250705A JP 25070589 A JP25070589 A JP 25070589A JP H0437151 B2 JPH0437151 B2 JP H0437151B2
Authority
JP
Japan
Prior art keywords
alloy
weight
solderability
lead
precipitated particles
Prior art date
Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
Expired - Lifetime
Application number
JP1250705A
Other languages
Japanese (ja)
Other versions
JPH0310036A (en
Inventor
Michiharu Yamamoto
Susumu Kawauchi
Masahiro Tsuji
Original Assignee
Nippon Mining Co
Priority date (The priority date is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the date listed.)
Filing date
Publication date
Application filed by Nippon Mining Co filed Critical Nippon Mining Co
Priority to JP25070589A priority Critical patent/JPH0310036A/en
Publication of JPH0310036A publication Critical patent/JPH0310036A/en
Publication of JPH0437151B2 publication Critical patent/JPH0437151B2/ja
Granted legal-status Critical Current

Links

Landscapes

  • Lead Frames For Integrated Circuits (AREA)
  • Conductive Materials (AREA)

Description

【発明の詳細な説明】[Detailed description of the invention]

〔産業上の利用分野〕 本発明は、トランジスタや集積回路(IC)な
どの半導体機器のリード材に適する銅合金に関す
るものである。 〔従来技術と問題点〕 従来、半導体機器のリード材としては、熱膨張
係数が低く、素子およびセラミツクスとの接着お
よび封着性の良好なコバール合金、42合金などの
高ニツケル合金が好んで使われてきた。 しかし、近年、半導体回路の集積度の向上に伴
い、消費電力の高いICが多くなつてきたため、
使用されるリード材も放熱性、熱伝導性が良好な
銅基合金が使われるようになつてきた。 しかし、リード材としては、熱伝導性が良い、
耐熱性が良い、半田付け性、めつき密着性が良
い、強度が高い、耐食性がある、廉価である等の
広範な諸条件を全て満足する必要がある。 〔問題点を解決するための手段〕 そこで本出願人は、先に安価で諸特性が優れた
銅合金を開発した(特願昭55−183967→特開昭57
−109357、特願昭56−1630→特開昭57−116738)
が、本合金は析出硬化型合金であるため、マトリ
ツクスに析出物を生成させ、強度、熱伝導性を共
に改善しようとするものである。 しかし、析出物の存在は必ずしも特性改善に寄
与するとはかぎらず、特に半田付け性、めつき密
着性にとつては有害なものとなり得る。 近年、表面実装の進展が著しく、また、信頼性
の向上要求が一段と厳しくなつているため、半田
付け性、めつき密着性の改善が強く求められてい
る。 また、半導体の集積度の向上にともない、リー
ドフレームのピン数が増加してきているのが現状
である。 従つて、プレス、エツチングといつたリード材
の加工性も一段と厳しくなつており、析出硬化型
合金はこの観点からも問題があつた。 そこで、本発明は、この合金を半導体機器のリ
ード材として用いるには、析出粒子の大きさを厳
密に調整する必要があり、特に、半田付け性、め
つき密着性を良好にするには、析出粒子を5μm以
下にする必要があることを見出した。 そして本発明は、ニツケル0.4〜2.9重量%、け
い素0.1〜0.725重量%、銅及び不可避不純物から
なるリード材用銅合金の析出粒子が5μm以下であ
る半導体機器用リード材に関する。 本発明に係る合金は、リード材に要求される放
熱性、耐熱性、強度、半田付け性、めつき密着性
等のすべてが良好なるものである。 〔発明の具体的な説明〕 次に、合金成分の限定理由を説明する。ニツケ
ルの含有量を0.4〜2.9重量%とする理由はニツケ
ルの含有量が0.4重量%未満では、けい素を0.1重
量%以上添加しても高強度でかつ高導電性を示す
合金が得られず、逆にニツケル含有量が2.9重量
%を超えると加工性が低下し、半田付け性も低下
する為である。 けい素含有量を0.1〜0.725重量%とした理由
は、けい素含有量が0.1重量%未満ではニツケル
を0.4重量%以上添加しても高強度でかつ高導電
性を示す合金が得られず、けい素含有量が0.725
重量%を超えると加工性、導電性の低下が著しく
なり、また半田付け性も低下する為である。 析出粒子を5μm以下にした理由は、5μmを超え
ると析出粒子上に半田めつきが良好につかず半田
付け性、めつき密着性が低下し、さらにはプレス
時に金型の型摩耗を起こしたり、エツチング面が
析出物脱落等による荒れが生じるといつた加工性
が低下するためである。 以下、実施例について説明する。 〔実施例〕 第1表に示した組成の合金を溶解し、厚さ100
mmの鋳塊を得た。次に鋳塊を約800℃で熱間圧延
し、厚さ7.5mmにした後、表面を面削する。そし
て冷間圧延で厚さ1.5mmにした後800℃で5分焼鈍
し、最終冷間圧延で0.8mmにし、420℃で6時間熱
処理する。 なお、比較合金については時効処理等の条件を
変えることによつて析出粒子が第1表に示すよう
に粗大化したものである。 この試料を5重量%の硫酸で約10秒間酸洗し、
引張強さ、伸び、硬さを測定した。また半田付け
性は垂直式浸漬法で230℃の半田浴(スズ60−鉛
40)に5秒間浸漬し、ハンダのぬれの状態を目視
観察した。まためつき密着性は、材料表面に、め
つき厚さ5μm程度銀めつきし350℃で5分間加熱
し、放冷後目視にてふくれの有無で評価した。 第1表に示す如く本発明に係る合金1〜6は、
析出粒子が5μm以下で有り比較合金1〜4と比べ
ると、半導体機器のリード材として十分な強度を
具え、半田付け性、めつき密着性が良好であるた
め、半導体機器のリード材として優れた合金であ
ることがわかる。 [発明の効果] 本発明合金は優れた強度を具備し、また、リー
ドフレーム材として使用する際のポイントとなる
信頼性を低下させないという前提に対して重要な
技術項目である半田付け性、めつき密着性が著し
く良好な合金である。
[Industrial Application Field] The present invention relates to a copper alloy suitable as a lead material for semiconductor devices such as transistors and integrated circuits (ICs). [Prior art and problems] Traditionally, high nickel alloys such as Kovar alloy and 42 alloy have been preferred as lead materials for semiconductor devices because of their low coefficient of thermal expansion and good adhesion and sealing properties with elements and ceramics. It has been. However, in recent years, as the degree of integration of semiconductor circuits has improved, the number of ICs with high power consumption has increased.
Copper-based alloys, which have good heat dissipation and thermal conductivity, have come to be used as lead materials. However, as a lead material, it has good thermal conductivity.
It is necessary to satisfy a wide range of conditions such as good heat resistance, good solderability, good plating adhesion, high strength, corrosion resistance, and low price. [Means for solving the problem] Therefore, the present applicant first developed a copper alloy that was inexpensive and had excellent properties (Japanese Patent Application No. 55-183967 → Japanese Unexamined Patent Publication No. 57-1983).
−109357, Patent application 1986-1630→Patent application 1984-116738)
However, since this alloy is a precipitation hardening alloy, it is intended to improve both strength and thermal conductivity by forming precipitates in the matrix. However, the presence of precipitates does not necessarily contribute to the improvement of characteristics, and can be particularly harmful to solderability and plating adhesion. In recent years, there has been significant progress in surface mounting, and demands for improved reliability have become even stricter, so there is a strong demand for improvements in solderability and plating adhesion. Furthermore, as the degree of integration of semiconductors increases, the number of pins on lead frames is currently increasing. Therefore, the processability of lead materials, such as pressing and etching, has become even more difficult, and precipitation hardening alloys have had problems from this point of view as well. Therefore, in the present invention, in order to use this alloy as a lead material for semiconductor devices, it is necessary to strictly adjust the size of precipitated particles, and in particular, in order to improve solderability and plating adhesion, It was found that it is necessary to reduce the size of precipitated particles to 5 μm or less. The present invention also relates to a lead material for a semiconductor device in which the precipitated particles of a copper alloy for a lead material, which is composed of 0.4 to 2.9% by weight of nickel, 0.1 to 0.725% by weight of silicon, copper, and unavoidable impurities, are 5 μm or less. The alloy according to the present invention has good heat dissipation, heat resistance, strength, solderability, plating adhesion, etc. all required for lead materials. [Specific Description of the Invention] Next, the reasons for limiting the alloy components will be explained. The reason for setting the nickel content to 0.4 to 2.9% by weight is that if the nickel content is less than 0.4% by weight, an alloy with high strength and high conductivity cannot be obtained even if silicon is added at 0.1% by weight or more. Conversely, if the nickel content exceeds 2.9% by weight, processability and solderability will decrease. The reason for setting the silicon content to 0.1 to 0.725% by weight is that if the silicon content is less than 0.1% by weight, even if 0.4% by weight or more of nickel is added, an alloy with high strength and high conductivity cannot be obtained. Silicon content is 0.725
This is because if the content exceeds % by weight, workability and conductivity will be significantly reduced, and solderability will also be reduced. The reason for setting the precipitated particles to be 5 μm or less is that if the precipitated particles exceed 5 μm, solder plating will not adhere well to the precipitated particles, resulting in poor solderability and plating adhesion, and furthermore, mold wear during pressing may occur. This is because when the etched surface becomes rough due to falling off of precipitates, the workability deteriorates. Examples will be described below. [Example] An alloy having the composition shown in Table 1 was melted to a thickness of 100 mm.
An ingot of mm was obtained. Next, the ingot is hot rolled at approximately 800℃ to a thickness of 7.5mm, and then the surface is face-milled. Then, it is cold rolled to a thickness of 1.5 mm, annealed at 800°C for 5 minutes, finally cold rolled to 0.8 mm, and heat treated at 420°C for 6 hours. As for the comparative alloys, the precipitated particles were coarsened as shown in Table 1 by changing the aging treatment and other conditions. This sample was pickled with 5% by weight sulfuric acid for about 10 seconds,
Tensile strength, elongation, and hardness were measured. In addition, solderability was tested using a vertical immersion method in a 230°C solder bath (tin 60-lead).
40) for 5 seconds and visually observed the state of solder wetting. The plating adhesion was evaluated by silver plating the material surface to a thickness of approximately 5 μm, heating it at 350° C. for 5 minutes, and visually observing the presence or absence of blisters after cooling. As shown in Table 1, alloys 1 to 6 according to the present invention are:
The precipitated particles are less than 5μm, and compared to Comparative Alloys 1 to 4, it has sufficient strength as a lead material for semiconductor devices, and has good solderability and plating adhesion, making it an excellent lead material for semiconductor devices. It can be seen that it is an alloy. [Effects of the invention] The alloy of the present invention has excellent strength, and also has excellent solderability and mechanical properties, which are important technical items based on the premise that reliability, which is a key point when used as a lead frame material, does not deteriorate. This alloy has extremely good adhesion.

【表】【table】

【表】【table】

Claims (1)

【特許請求の範囲】 1 ニツケル;0.4〜2.9重量%、 けい素;0.1〜0.725重量%、 銅及び不可避不純物;残 からなるリード材用銅合金の析出粒子が5μm以下
である半導体機器用リード材。
[Scope of Claims] 1. A lead material for a semiconductor device in which the precipitated particles of a copper alloy for a lead material are 5 μm or less, comprising: nickel; 0.4 to 2.9% by weight; silicon; 0.1 to 0.725% by weight; copper and unavoidable impurities; the remainder; .
JP25070589A 1989-09-28 1989-09-28 Lead material for semiconductor apparatus Granted JPH0310036A (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
JP25070589A JPH0310036A (en) 1989-09-28 1989-09-28 Lead material for semiconductor apparatus

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP25070589A JPH0310036A (en) 1989-09-28 1989-09-28 Lead material for semiconductor apparatus

Related Parent Applications (1)

Application Number Title Priority Date Filing Date
JP57006063A Division JPS6045698B2 (en) 1982-01-20 1982-01-20 Lead material for semiconductor equipment

Publications (2)

Publication Number Publication Date
JPH0310036A JPH0310036A (en) 1991-01-17
JPH0437151B2 true JPH0437151B2 (en) 1992-06-18

Family

ID=17211820

Family Applications (1)

Application Number Title Priority Date Filing Date
JP25070589A Granted JPH0310036A (en) 1989-09-28 1989-09-28 Lead material for semiconductor apparatus

Country Status (1)

Country Link
JP (1) JPH0310036A (en)

Families Citing this family (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US5178493A (en) * 1989-11-16 1993-01-12 Societe Civile Des Brevets De Henri Vidal Counterfort wall
JP4494258B2 (en) * 2005-03-11 2010-06-30 三菱電機株式会社 Copper alloy and manufacturing method thereof
JP5452060B2 (en) * 2009-04-03 2014-03-26 三菱電機株式会社 Copper alloy and manufacturing method thereof

Family Cites Families (5)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US307250A (en) * 1884-10-28 Safe-lock for toy banks
US2137282A (en) * 1938-08-12 1938-11-22 Mallory & Co Inc P R Copper alloys
GB522482A (en) * 1938-11-28 1940-06-19 Mallory & Co Inc P R Improvements in and relating to the production of copper base alloys
JPS5834536B2 (en) * 1980-06-06 1983-07-27 日本鉱業株式会社 Copper alloy for lead material of semiconductor equipment
JPS5895850A (en) * 1981-12-02 1983-06-07 Kobe Steel Ltd Copper alloy for lead frame of integrated circuit

Also Published As

Publication number Publication date
JPH0310036A (en) 1991-01-17

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